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dc.contributor.authorKyriakides, George K.en
dc.contributor.authorArora, V. K.en
dc.contributor.authorLifton, J.en
dc.contributor.authorNuttall, F. Q.en
dc.contributor.authorMiller, Jody C.en
dc.creatorKyriakides, George K.en
dc.creatorArora, V. K.en
dc.creatorLifton, J.en
dc.creatorNuttall, F. Q.en
dc.creatorMiller, Jody C.en
dc.date.accessioned2018-06-22T09:53:52Z
dc.date.available2018-06-22T09:53:52Z
dc.date.issued1976
dc.identifier.urihttps://gnosis.library.ucy.ac.cy/handle/7/42069
dc.description.abstractSegmental duct ligated pancreatic allografts were performed in pigs. Control untreated grafts underwent significant destruction secondary to inflammation and rejection within 2 weeks following transplantation. Treatment with Solu-Medrol prevented these changes and preserved both the endocrine and the exocrine functions of the allografts. Because of continuing exocrine function, however, large quantities of amylase-rich peripancreatic fluid accumulated and became secondarily infected. Addition of glucagon to this regimen significantly inhibited exocrine pancreatic function and thus prevented fluid accumulation and peripancreatic abscess formation. The additional effect of azathioprine on these grafts was minimal. In conclusion, Solu-Medrol prevents the inflammation, fibrosis, and rejection of duct ligated pancreatic allografts but allows large quantities of amylase-rich peripancreatic fluid to accumulate and become infected. This can be prevented by glucagon, which inhibits the exocrine pancreatic function. © 1976.en
dc.language.isoengen
dc.sourceJournal of Surgical Researchen
dc.titlePorcine pancreatic transplants II. Allotransplantation of duct ligated segmentsen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1016/0022-4804(76)90120-7
dc.description.volume20
dc.description.issue5
dc.description.startingpage461
dc.description.endingpage466
dc.author.facultyΙατρική Σχολή / Medical School
dc.author.departmentΙατρική Σχολή / Medical School
dc.type.uhtypeArticleen


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